HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 2-Hydroxymuconic semialdehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Ampicillin | HCID 6249 | — |
| Reactant | HCID 178418840 | HCID 178418840 | — |
| Product | 2-Hydroxymuconic semialdehyde | HCID 5280366 | — |
Reaction Steps
Screening for transformants carrying pheA and pheB. Transformants were spread on LB plates containing 1 mM phenol, 50 μg of ampicillin per ml, and 12.5 μg of tetracycline per ml and incubated overnight at 37° C. Colonies that became yellow (as a result of 2-hydroxymuconic semialdehyde) following spraying of a 0.1% of catechol solution were patched on LB plates containing 1 mM phenol. Colonies in which the yellow compound formed during growth without catechol addition were retained as putative carriers of both pheA and pheB.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834297 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-8c85ce7f760f497c8a7c99cabcfa91b2 |
| Source note | uspto-grants-1998_11 |